EP0830314B1 - Porous inorganic oxide materials prepared by non-ionic surfactant templating route - Google Patents
Porous inorganic oxide materials prepared by non-ionic surfactant templating route Download PDFInfo
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- EP0830314B1 EP0830314B1 EP96916589A EP96916589A EP0830314B1 EP 0830314 B1 EP0830314 B1 EP 0830314B1 EP 96916589 A EP96916589 A EP 96916589A EP 96916589 A EP96916589 A EP 96916589A EP 0830314 B1 EP0830314 B1 EP 0830314B1
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- C01B37/005—Silicates, i.e. so-called metallosilicalites or metallozeosilites
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- C01F7/02—Aluminium oxide; Aluminium hydroxide; Aluminates
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Definitions
- This invention relates to the synthesis of crystalline, porous inorganic oxide materials possessing uniform framework-confined mesopores in the range 2.0-10.0 nm and large elementary particle size of greater than 500 nm.
- the present invention relates to such materials where the formation of the mesoporous structure is accomplished by a novel self-assembly mechanism involving complexation and/or hydrogen (H) bonding between aqueous or alcoholic emulsions of various nonionic polyethylene oxide based surfactants (N°) and various neutral inorganic oxide precursors (I°). This is followed by hydrolysis and subsequent condensation of hydrolysis products at ambient reaction temperatures.
- H complexation and/or hydrogen
- This (N°I°) templating approach allows for the removal of template through calcination or solvent extraction which lowers material and energy costs.
- the template is biodegradable.
- the (N°I°) templating approach also affords non-lamellar mesostructures of metal oxides in addition to silica.
- Porous materials may be structurally amorphous, para-crystalline or crystalline.
- Amorphous materials such as silica gel or alumina gel, do not possess long range crystallographic order, whereas para-crystalline solids such as ⁇ - or ⁇ - alumina are semi-ordered, producing broad X-ray diffraction peaks.
- Both these classes of materials exhibit very broad pore distributions predominantly in the mesoporous range. This wide pore distribution however, limits the effectiveness of catalysts, adsorbents and ion-exchange systems prepared from such materials.
- Zeolites and some related molecular sieves such as; alumino-phosphates and pillar interlayered clays, possess rigorous uniform pore sizes.
- Zeolites are considered as a subclass of molecular sieves owing to their ability to discriminate small molecules and perform chemistry upon them.
- Molecular sieves in general are materials with crystalline frameworks in which tetrahedral Si and/or Al atoms of a zeolite or zeolitic lattice are entirely or in part substituted by other atoms such as B, Ga, Ge, Ti, Zr, V, Fe or P.
- Negative charge is created in the zeolite framework by the isomorphous substitution of Si 4+ ions by Al 3+ or similar ions. In natural zeolites, this charge is balanced by the incorporation of exchangeable alkali or alkaline earth cations such as Na + , K + , Ca 2+ .
- Synthetic zeolites utilize these and other cations such as quaternary ammonium cations and protons as charge balancing ions.
- Zeolites and molecular sieves are generally prepared from aluminosilicate or phosphate gels under hydrothermal reaction conditions. Their crystallization, according to the hereafter discussed prior art, is accomplished through prolonged reaction in an autoclave for 1-50 days and oftentimes, in the presence of structure directing agents (templates). The correct selection of template is of paramount importance to the preparation of a desired framework and pore network.
- templates structure directing agents
- 3,702,886 teaches that an aluminosilicate gel (with nigh Si/Al ratio) crystallized in the presence of quaternary tetrapropyl ammonium hydroxide template to produce zeolite ZSM-5.
- Other publications teach the use of different organic templating agents and include; U. S. Pat. No. 3,709,979, wherein quaternary cations such as tetrabutyl ammonium or tetrabutyl phosphonium ions crystallize ZSM-11 and U. S. Pat. No. 4,391,785 demonstrates the preparation of ZSM-12 in the presence of tetraethyl ammonium cations.
- Pathway 2 Hexagonal iron and lead oxide and lamellar lead and aluminum oxide phases have been reported using Pathway 2 (Stucky et al. ibid .).
- Pathway 3 The viability of Pathway 3 was demonstrated by the synthesis of hexagonal MCM-41 using a quaternary alkyl ammonium cation template under strongly acidic conditions (5 - 10 mol L -1 HCl or HBr) in order to generate and assemble positively charged framework precursors (Stucky et al. ibid ).
- Pathway 4 was demonstrated by the condensation of anionic aluminate species with an anionic template (C 12 H 25 OPO 3 - ) via alkali cation mediated (Na + , K + ) ion pairing, to produce a lamellar Al(OH) 3 phase. Pinnavaia et al.
- Framework-confined uniform pores are pores formed by the nucleation and crystallization of the framework elementary particles and are typically highly regular cavities and channels confined by the solid framework. The size of these cavities and channels is predetermined by the thermodynamically favored assembly routes.
- Textural porosity is that which can be attributed to voids and channels between elementary particles and/or aggregates of such particles (grains). Each elementary particle in the case of molecular sieves is composed of a certain number of framework unit cells each in turn containing framework-confined uniform pores. Textural porosity is formed during crystal growth and segregation or during subsequent thermal treatment or acid leaching.
- the size of the textural pores is determined by the size, shape and the number of interfacial contacts of these particles or aggregates.
- the size of the textural pores is generally one or two orders of magnitude larger than that of the framework-confined pores and is proportional to the elementary particle size.
- XRD powder X-ray diffraction
- SEM Scanning Electron Microscopy
- TEM Transmission Electron Microscopy
- adsorption/desorption can determine the existence of and differentiate between framework-confined and textural mesoporosities.
- the crystallographic distance between repeat units in the elementary particles and some information about the arrangement of such repeat units can be obtained from XRD.
- Particle sizes and shapes and preliminary information regarding textural mesoporosity can be established by SEM and TEM.
- Analysis of the N 2 or Ar adsorption-desorption isotherms of the solid material can indicate both framework-confined and textural mesoporosities.
- Textural mesoporosity is evidenced by the presence of a Type IV isotherm exhibiting a well defined hysteresis loop in the relative pressure region P i / P 0 > 0.5 (Sing et al., Pure Appl. Chem ., Vol. 57, 603-619, (1985)). This behavior is common for a variety of para-crystalline materials and freeze-dried pillared layered solids.
- Framework-confined mesoporosity is characterized by a sharp adsorption uptake followed by a hysteresis loop in the 0.3-0.4 P i / P 0 region. This hysteresis corresponds to capillary condensation in the framework-confined mesopores.
- the large particle size precludes the formation of textural mesoporosity and a corresponding ratio of textural to framework-confined mesoporosity approaching zero is calculated.
- the elementary particle size was smaller ( ⁇ 40.0 nm) producing a ratio of textural to framework-confined mesoporosity greater than 0.2.
- the molecular sieve materials and preparation techniques provide several distinct disadvantages and advantages:
- Figures 1A and 1B are graphs showing representative X-ray powder diffraction patterns of MCM-41 (Fig. 1A) Beck et al., J. Am. Chem. Soc., Vol. 114, 10834 - 10843, (1992) and HMS (Fig. 1B) Pinnavaia et al. ( Science , Vol. 267, 865 - 867, (1995) products .
- Figures 2A and 2B are graphs showing representative N 2 adsorption-desorption isotherm for MCM-41 (Fig. 2A) Beck et al., J. Am. Chem. Soc ., Vol. 114, 10834 - 10843, (1992) and HMS (Fig. 2B) Pinnavaia et al. ( Science , Vol. 267, 865 - 867, (1995) products .
- Figure 3 is a graph showing the X-ray powder diffraction patterns of the as synthesized (curve A) and calcined (curve B) MSU-1 products from Example 3.
- Figure 4 is a graph of the N 2 adsorption-desorption isotherm for the calcined MSU-1 product from Example 3.
- Figure 4A is a graph of the corresponding Horvath-Kawazoe framework-confined mesopore size distribution curve.
- Figure 5 is a graph of the X-ray powder diffraction patterns of the as synthesized (curve A) and calcined (curve B) MSU-3 products from Example 16.
- Figure 6 is a graph of the N 2 adsorption-desorption isotherm for the calcined MSU-3 product from Example 16.
- Figure 6A is a graph of the corresponding Horvath-Kawazoe framework-confined mesopore size distribution curve.
- Figure 7 is a graph of the X-ray powder diffraction patterns of the as-synthesized (curve A) and calcined (curve B) MSU-3 Alumina products of Example 19.
- Figure 8 is a graph of the N 2 adsorption-desorption isotherm for the calcined MSU-3 Alumina product from Example 19.
- Figure 8A is a graph of the corresponding Horvath-Kawazoe framework-confined mesopore size distribution curve.
- Figure 9 is a representative chemical structure of a secondary fatty alcohol poly-ethoxylate (TergitolTM).
- Figure 10A is a representative chemical structure of an alkyl phenol poly-ethoxylate (Triton XTM).
- Figure 10B is Igepal RC-760.
- Figure 11 is a representative chemical structure of a fatty acid ethoxylate.
- Figure 12 is a representative chemical structure of an ethylene oxide-propylene oxide-ethylene oxide tri-block co-polymer (Pluronic 64LTM).
- Figure 13 is a representative chemical structure of the ethylene diamine propylene oxide-ethylene oxide derivative (TetronicTM).
- Figure 14 is a representative chemical structure of a primary fatty amine poly-ethoxylate.
- Figure 15 is a representative chemical structure of a fatty acid PPO/PEO block co-polymer.
- Figure 16 is a representative chemical structure of a sorbitan ethoxylate.
- the present invention relates to a synthetic, semi-crystalline inorganic oxide composition having at least one resolved x-ray reflection corresponding to a lattice spacing of 3 to 10 nm, a framework wall thickness of at least about 2 nm, framework confined pores between about 2 and 10 nm, an elementary particle size greater than 500 nm, and a specific surface area of 300 to 1200 square meters per gram.
- the present invention also relates to a synthetic, semi-crystalline inorganic oxide composition prepared by reacting in a reaction mixture a nonionic poly(alkylene oxide) derived surfactant as a template (N°) and a neutral inorganic oxide precursor (I°), followed by hydrolysis and crosslinking of the inorganic oxide precursor to provide the composition.
- the present invention further relates to a method for the preparation of a synthetic semi-crystalline inorganic oxide composition which comprises: providing a mixture of (i) a neutral inorganic oxide precursor (I°) containing at least one element selected from the group consisting of di-, tri-, tetra-, penta- and hexavalent elements and mixtures thereof; (ii) a non-ionic poly(alkylene oxide) surfactant (S°) as a template; and (iii) a hydrolyzing agent; mixing the solution to form a gel containing the composition; separating at least some of the hydrolyzing agent and the surfactant to form the composition; and optionally calcining the composition.
- a neutral inorganic oxide precursor I°
- S° non-ionic poly(alkylene oxide) surfactant
- the present invention provides to a new route to the synthesis of semi-crystalline materials with well defined framework-confined mesopores and large elementary particle size.
- the compositions produced in the current invention are distinguished from those of the prior art by the virtue of the method of preparation of the present invention, the subsequent architecture of the mesoporous structure and the range of templated metal oxides other than silica that is afforded by this route.
- Formation of the mesoporous network is accomplished by interaction (complexation and/or hydrogen-bonding) between a nonionic polyethylene oxide based surfactant template and neutral inorganic precursors, followed by hydrolysis and subsequent condensation of the inorganic reaction product under either ambient or elevated temperature reaction conditions and the subsequent removal of the solvent phase and the template.
- the present invention particularly provides a preferred totally nonionic (N • I • ) route to the preparation of quasi-crystalline oxide compositions
- a preferred totally nonionic (N • I • ) route to the preparation of quasi-crystalline oxide compositions comprising (a) preparing a homogeneous solution or emulsion of a nonionic polyethylene oxide-based surfactant (N • ) by stirring, sonicating or shaking at standard temperature and pressure (STP); (b) addition of one or more neutral inorganic precursors with stirring at standard temperatures and pressures (STP) to the emulsion of step (a) at ambient temperature to form a precipitated semi-crystalline product; (c) separating the solvent and the hydrolyzing agent from the precipitated product by filtration or centrifugation; (d) optionally calcining the quasi-crystalline product at 673°K to 873° K for at least 4 hours in air or (e) extracting the template through solvent extraction whereby the solvent is either water or ethanol.
- the present invention thus provides a new route to inorganic oxide crystalline materials with uniform well defined framework-confined mesopores and controlled elementary particle size that can be utilized as adsorbents, catalysts and catalyst supports for the catalytic conversion of organic substrates.
- the present invention is distinguished from the prior art by the new preparative N • I • method used to obtain the mesoporous crystalline inorganic oxide materials, the pore morphology of the said materials and the range of templated mesoporous metal oxide materials that may be prepared by this method.
- the formation of the mesoporous structure is accomplished by interaction (complexation and/or hydrogen bonding) between template molecules within micellar aggregates of nonionic polyethylene oxide-based templates and neutral inorganic oxide precursors, followed by hydrolysis and cross linking of IO x units, where I is a central metallic or non-metallic element coordinated to x oxygen atoms (2 ⁇ x ⁇ 6).
- This interaction is most likely to occur between an I-OH unit and the terminal OH function of each surfactant molecule, or between the I-OH unit and the array of lone pair electrons on the template polar segment.
- the polar segment of the template in the present invention is flexible and appears to act in the fashion of a crown ether complexing a I-OH unit, thereby stabilizing a site of nucleation for subsequent condensation of the mesoporous quasi-crystalline inorganic oxide product, although the inventors do not want to be bound to any particular theory.
- the inventors know of no prior art teaching the preparation of micro-, meso-, or macro-porous inorganic oxide compositions by such a nonionic N • I° mechanism involving crystallization of inorganic oxide precursors around well defined micelles of nonionic surfactants.
- the present result is achieved by using micelles of a nonionic surfactant to template and assemble a neutral inorganic reactant precursor into a mesoporous framework structure.
- Complexation and/or hydrogen bonding between the template and the reagent is believed to be the primary driving force of the assembly of the framework in the current invention.
- the aforementioned method consists of the formation of a solid precipitate by the mixing of a solution or emulsion of a polyethylene oxide-based nonionic surfactant, with a neutral inorganic oxide precursor.
- a polyethylene oxide-based nonionic surfactant being an inorganic alkoxide
- the template may be recovered by extraction with ambient temperature alcohol or hot water whose temperature exceeds the cloud point of the template. Complete removal of the remainder of the template and final crosslinking of the IO x framework is accomplished by calcination in air at temperatures between 673° K and 923° K for at least 4 h.
- the molar ratio of inorganic oxide precursor to surfactant is between 10:1 and 20:1 depending upon the specific template being used.
- the concentration of surfactant in solution is between 0.003 mol L -1 and 0.4 mol L -1 again depending upon the surfactant being used and the pore size desired.
- the crystalline inorganic oxide composition of the present invention in its calcined state has the desired composition: nR-EO/A v B w C x D y O z
- R-EO is at least one of a selection of nonionic alkyl, or alkyl/aryl polyethylene oxide or polyethylene oxide-polypropylene oxide-polyethylene oxide block co-polymer molecules
- A is at least one optional trivalent element such as Al, Ga or Fe
- B is at least one optional tetravalent metallic element such as Ge, Ti, V, Sb or Zr
- C is the optional tetravalent element Si
- D is an optional pentavalent or hexavalent element such as V, W or Mo
- O is oxygen and v, w, x, y and z are the molar stoichiometries of A, B, C, D and O respectively.
- the semi-crystalline mesoporous materials of the present invention may be described as being formed by hydrogen-bonding between the terminal hydroxyl function or the array of lone pair electrons on the O atoms of the ethylene oxide units of the template molecules and any M-(OR) x compound. This H-bonding is followed by hydrolysis and subsequent condensation and cross-linking of IO x units under ambient or elevated temperature reaction conditions.
- composition of this invention is characterized by at least one strong XRD peak at a basal (d 100 ) spacing of at least 3.0 nm or larger.
- the compositions are also distinguished in part from those of the prior art, specifically MCM-41 materials, by lower crystallographic regularity and larger framework wall thicknesses ( ⁇ 2.0 nm).
- the composition of the present invention is distinguished from the prior art of HMS materials by lower crystallographic regularity, the presence of longer range pore structures, substantially larger particle sizes and near zero textural mesoporosity.
- the template may be removed from the condensed reaction products in at least three different ways: (i) air drying followed by calcination in air or in inert gas preferably at a temperature from 673° K to 923° K for 4 to 6 h; (ii) solvent extraction of the template from the air dried material using alcohol or hot water; (iii) combination of (i) and (ii).
- Procedure (i) results in the complete oxidation and thereby decomposition of the occluded template.
- the current invention improves on the environmental impact of the prior material preparation art, as the oxidation products of quaternary ammonium and amine based surfactant templates described in the prior art, include environmentally undesirable NO x gases, while the oxidation products of polyethylene oxide based surfactants are the more environmentally compatible H 2 O and CO 2 gasses.
- Procedure (ii) allows the template to be recovered and subsequently recycled and reused. If the template is removed by procedure (ii), the product should be calcined in air or inert gas to remove the final traces of the template and to complete the cross linking of the mesostructure.
- the present compositions may be used as adsorbents, molecular sieves, catalysts and catalyst supports.
- a catalytically active element such as Al, Ag, Cu, Cr, Pt, Pd, Ti, V, Zr or mixtures thereof, or when intercalated with transition metal inorganic metallocycles, it can be used as a catalyst for cracking, hydrocracking, hydrogenation-dehydrogenation, isomerization or oxidations involving large and small organic substrates.
- the new synthesis method of the compositions of this invention involves the preparation of solutions or emulsions of a surfactant template compound and reaction of this solution with liquid di-, tri-, tetra-, penta- or hexa-valent metal or metalloid hydrolyzable reagents in the presence of a hydrolysing agent under stirring, sonication or shaking, until formation of the desired precipitated product is achieved and recovering the solid material.
- the template is described more particularly as a nonionic (neutral) polyethylene oxide based molecule that would possess one of many different molecular structures and the hydrolysing agent is described as water.
- alkyl-polyethylene oxides such as are related to the Tergitol 15-S- m products ( Figure 9) are derived from the reaction of ethylene oxide with a primary or secondary alcohol and possess the basic formula R n -O(EO) m H where R is a hydrophobic alkyl group with n ranging from 1 to at least 20 carbon atoms, EO is a hydrophilic ethylene oxide unit (OCH 2 CH 2 ) with m ranging from about 7 to 40, preferably at least 20.
- R is a hydrophobic alkyl group with n ranging from 1 to at least 20 carbon atoms
- EO is a hydrophilic ethylene oxide unit (OCH 2 CH 2 ) with m ranging from about 7 to 40, preferably at least 20.
- alkyl-phenyl polyethylene oxides such as Igepal-RC ( Figure 10B) and Triton-X ( Figure 10A) possess the same range of structures as the alkyl-polyethylene oxides, with the exception that the primary (Igepal RC), secondary or tertiary (Triton X) R group is bound to the EO units through a hydrophobic phenoxy group (PhO).
- These molecules then, have the basic formula; R n -Ph-O(EO) m H, preferably where m is 8 to 10 and n is 8.
- the polyethylene oxide (PEO)-polypropylene oxide (PPO) molecules are derived from the addition of hydrophobic propylene oxide to propylene glycol followed by the addition of hydrophilic ethylene oxide. They are defined as PEO n -PPO m -PEO n tri-block co-polymers wherein n is controlled by length to constitute from 10% to 80% by weight of the final product. The order of the PEO and PPO units may be reversed in order to produce the PPO m -PEO n -PPO m triblock co-polymers; Pluronic-R.
- n is 30 and m is 13.
- a fourth basic PEO based surfactant type is derived by from the substitution of the hydrogens of ethylene diamine by ethylene oxide and propylene oxide units to form the X shaped, Tetronic, molecules ( Figure 13) with basic formula; ((EO) n -(PO) m ) 2 -NCH 2 CH 2 N-((PO) m -(EO) n ) 2 .
- the order of the PEO and PPO groups in these molecules may also be reversed to form Tetronic-R.
- m is 13 and n is 30.
- compositions comprise steps as follows:
- the inorganic oxide precursors are single or double metal alkoxide compounds,
- the list of preferred alkoxides includes but not exclusively: aluminum(III) ethoxide, aluminum(III) isopropoxide, aluminum(III) n -, sec- or tert- butoxide, antimony(III) isopropoxide, antimony(III) n -butoxide, calcium(II) ethoxide, calcium(II) isopropoxide, calcium(II) tert - butoxide, chromium(IV) isopropoxide, chromium(IV) tert - butoxide, copper(II) methoxyethoxide, gallium(III) isopropoxide, germanium(IV) ethoxide, germanium(IV) isopropoxide, indium(III) isopropoxide, iron(III) ethoxide, iron(III) isopropoxide, iron(III) tert - butoxide, lead
- the alcohols used in step (i) of the preparation art correspond to the alcoholate ligand from which the metal alkoxide is derived.
- the alcohols thus preferred are methanol, ethanol, n- and isopropanol and n-, sec-, tert-, butanol.
- the alcohols contain 1 to 4 carbon atoms.
- Said mixed metal alkoxides are obtained through proprietary preparations or by reaction of desired metal alkoxides in desired molar ratios under reflux (433° K) for 3 - 4 h.
- the said reacting of the inorganic precursor and the template solution is achieved at room temperature (298° K to 303° K) under stirring for at least 16 h.
- Aging of the reaction mixture may be achieved at room temperature either under stirring, sonication or shaking or by being left to stand for at least 24 h. More specifically, the reacting occurs through complexation or H-bonding between a neutral nonionic template and neutral inorganic oxide precursors, followed by hydrolysis and crosslinking of IO x units at ambient or elevated reaction temperatures.
- the complexation, or H-bonding most likely occurs between the terminal OH group of the template molecules and the hydrolyzable ligand on the inorganic precursor molecule, or between the inorganic precursor molecule and the electron lone pairs of the ethylene oxide groups in the hydrophilic head group of the template molecules.
- the calcination is performed in a temperature controlled oven by heating in air at a rate of 2° K min -1 to a final temperature between 673° K and 923° K for at least 30 min, preferably 4 to 6 h.
- the templated inorganic oxide compositions of the present invention can be combined with other components, for example, zeolites, clays, inorganic oxides or organic polymers or mixtures thereof. In this way adsorbents, ion-exchangers, catalysts, catalyst supports or composite materials with a wide variety of properties may be prepared. Additionally, one skilled in the art may impregnate or encapsulate transition metal macrocyclic molecules such as porphyrins or phthalocyanines containing a wide variety of catalytically active metal centers.
- the surfaces of the compositions can be functionalized in order to produce catalytic, hydrophilic or hydrophobic surfaces.
- This functionalization can be introduced during the synthesis procedure by replacing the metal alkoxide precursor with alkyl metal alkoxide [MR(OR) x -1 ] reactants, or metal carboxylate reactants.
- the surfaces may be functionalized after synthesis by reaction with various chlorides, fluorides, sylisation or alkylating reagents.
- the resulting solution was stirred and aged for 16 h at room temperature. During the initial 1-3 h stirring, white templated products were observed as solid precipitates. The products were separated from the mother liquor through filtration or centrifugation and dried at room temperature. The template was then removed through calcination in air at 923° K for 4 h.
- the diffraction data were recorded by step scanning at 0.02 degrees of 2 theta, where theta is the Bragg angle and photon counting time of 1 sec step -1 .
- the d-spacings of the X-ray reflections of the samples were calculated in nm.
- Transmission electron micrographs were obtained on a JEOL JEM 100CX II (Japan) electron microscope by observing unmodified particles supported on carbon coated copper grids (400 mesh).
- the sample images were obtained using an accelerating voltage of 120 kV, a beam diameter of approximately 5mm and an objective lens aperture of 20 mm.
- the pore structures of said compositions were characterized by measuring N 2 adsorption-desorption isotherms using a Coulter 360CX (Florida) sorptometer. Isotherms were recorded at 70° K using a standard continuous sorption procedure. Before measurement, each sample was outgassed overnight at 323° K and 10 -6 Torr.
- Thermogravimetric analyses of the samples were performed under a flow of dry N 2 gas on a CAHN system thermogravimetric gas (TG) analyzer using a heating rate of 5° K min -1 .
- the amounts of each surfactant used in the examples 1-6, together with the corresponding physico-chemical parameters are summarized in Table 1. *The Material designation is MSU-1.
- Example 9 Example 10: 0.1 mol R n -(OCH 2 CH 2 ) 15 OH 0.1 mol R n -(OCH 2 CH 2 ) 15 OH 33 mol H 2 O. 29 mol H 2 O.
- Example 11 0.1 mol R n -(OCH 2 CH 2 ) 15 OH 20 mol H 2 O.
- the resulting precipitate was aged under stirring at room temperature for 16 h to obtain the templated product.
- the product was then transferred into sealed containers and heated at 373° K for a further 16 h.
- the crystalline product was then filtered, dried at room temperature and calcined at 923° K for 4 h to remove the occluded template.
- the physico-chemical properties of the calcined templated products are described in Table 2. *The Material designation is MSU-1.
- Example Template formula Amount of Template used (g) d 100 (nm) HK pore diameter (nm) BET Surface area (M 2 g -1 ) 7 Tergitol 1.0 4.3 2.0 655 15-S-15 8 Tergitol 5.0 3.6 2.0 465 15-S-15 9 Tergitol 10.0 3.9 2.0 515 15-S-15 10 Tergitol 15.0 4.0 2.2 890 15-S-15 11 Tergitol 25.0 5.5 2.5 700 15-S-15
- Aqueous solutions of Triton-X 100 and Triton-X 114 were prepared as in the manner of the preparation art of Examples 1 through 11.
- the concentration of template was 7.5% weight of surfactant per weight of solvent.
- Si(OC 2 H 5 ) 4 was added at once in the appropriate amount so that the Si : surfactant molar ratio was 10 : 1 as in the preparation art of Examples 1 through 11.
- the remainder of the synthesis was identical to the preparation art described in Examples 1 through 6.
- the calcined templated products exhibited XRD patterns, BET surface areas, HK pore size distributions and pore wall thicknesses as described in Table 3. *The Material designation is MSU-2.
- compositions prepared by templating with various concentrations of the nonionic surfactant Pluronic 64L are presented for compositions prepared by templating with various concentrations of the nonionic surfactant Pluronic 64L.
- This surfactant differs from those discussed in the prior examples in that the hydrophobic part of the surfactant molecule is based on propylene oxide units.
- the molecule is defined as a polyethylene oxide-polypropylene oxide- polyethylene oxide tri-block co-polymer.
- Aqueous solutions of Pluronic 64L with concentrations of 5%, 10% and 15% weight of surfactant per weight of solvent were prepared as in the preparation art of the previous examples 1 through 13.
- Si(OC 2 H 5 ) 4 was added at once in the appropriate amount so that the Si : surfactant molar ratio was 20 : 1.
- the remainder of the preparation was identical to the preparation art of examples 7 through 11.
- the calcined templated products exhibited physico-chemical properties as described in Table 4. *The Material designation is MSU-3.
- Example 17 demonstrates the viability of recovering the template from the inorganic structure prior to calcination through solvent extraction.
- a 0.05 g quantity of the air dried and heat treated at 373° K but non-calcined product of Example 14 is examined by thermogravimetric analysis (TGA) under N 2 gas flow at a heating rate of 5° K C min -1 .
- TGA thermogravimetric analysis
- One gram of the same air dried and non-calcined product of Example 14 is stirred in 100 milliliters of hot water ( ⁇ 363° K ) for 3 h.
- the product is then filtered and washed with a second and a third 100 milliliter volumes of hot water.
- the filtered product is then dried at room temperature for 16 h. This product is then analyzed by TGA and vibrational spectroscopy.
- This example demonstrates the ability of the present invention to prepare compositions whereby framework Si atoms have been substituted by different metal atoms, for example Ti.
- a substituted or polymerized metal alkoxide compound is formed by reaction of Si(OC 2 H 5 ) 4 with Ti(OCH(CH 3 ) 2 ) 4 such that the molar % of Ti for each composition was 0.5%, 1.0% and 5.0%.
- the appropriate amount of Ti(OCH(CH 3 ) 2 ) 4 is dissolved in the appropriate quantity of Si(OC 2 H 5 ) 4 under stirring.
- the resultant solution is then heated under reflux at the boiling point of the Si(OC 2 H 5 ) 4 (433° K) for 4 h.
- the solution is then cooled to room temperature and added to a solution of nonionic polyethylene oxide based surfactant in the appropriate ratio as taught in Examples 1 through 16.
- the preparation art then follows that of Examples 7 through 11.
- This example describes the preparation art of nonionic surfactant templated mesoporous aluminum oxide.
- the desired amount of Pluronic 64L was dissolved under stirring at room temperature in 50 milliliters of an alcohol corresponding to the alkoxide ligand of the aluminum alkoxide inorganic precursor, which in the present art, was sec -butanol.
- the appropriate amount of Al(OCH(CH 3 )CH 2 CH 3 ) 3 was then dissolved in that solution such that the Al : surfactant molar ratio was 10 : 1. No precipitation reaction was observed at this point.
- An aliquot of deionized H 2 O was dissolved in 10 milliliters of sec -butanol such that the H 2 O : Al molar ratio was 2 : 1. This solution was added very slowly to the Al/surfactant solution under stirring at room temperature.
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Description
nR-EO/AvBwCxDyOz
wherein R-EO is at least one of a selection of nonionic alkyl, or alkyl/aryl polyethylene oxide or polyethylene oxide-polypropylene oxide-polyethylene oxide block co-polymer molecules; A is at least one optional trivalent element such as Al, Ga or Fe; B is at least one optional tetravalent metallic element such as Ge, Ti, V, Sb or Zr; C is the optional tetravalent element Si; D is an optional pentavalent or hexavalent element such as V, W or Mo; O is oxygen and v, w, x, y and z are the molar stoichiometries of A, B, C, D and O respectively. In the calcined composition, n ≈ 0, 0.001 ≤ v ≤ 2, 0.001≤ w ≤ 1, 0.001≤ x ≤ 1, 0.001 ≤ y ≤ 2 and 2 ≤ z ≤ 6.
0.1 mol R n -(OCH2CH2) m OH
50 mol H2O
*The Material designation is MSU-1. | |||||
Example | Template formula | Amount of template used. (g) | d100 (nm) | HK pore diameter (nm) | BET Surface area (m2 |
1 | Tergitol | 5.15 | 4.4 | 2.2 | 900 |
15-S-7 | |||||
2 | Tergitol | 5.84 | 5.2 | 2.5 | 1010 |
15-S-9 | |||||
3 | Tergitol | 7.38 | 4.1 | 3.1 | 1005 |
15-S-15 | |||||
4 | Tergitol | 8.77 | 5.4 | 2.6 | 640 |
15-S-15 | |||||
5 | Tergitol | 10.79 | 7.8 | 4.8 | 605 |
15-S-20 | |||||
6 | Tergitol | 15.58 | 7.9 | 4.5 | 525 |
15-S-30 |
Example 7: | Example 8: |
0.1 mol R n -(OCH2CH2)15OH | 0.1 mol R n -(OCH2CH2)15OH |
492 mol H2O. | 98 mol H2O. |
Example 9: | Example 10: |
0.1 mol R n -(OCH2CH2)15OH | 0.1 mol R n -(OCH2CH2)15OH |
33 mol H2O. | 29 mol H2O. |
Example 11 | |
0.1 mol R n -(OCH2CH2)15 | |
20 mol H2O. |
*The Material designation is MSU-1. | |||||
Example | Template formula | Amount of Template used (g) | d100 (nm) | HK pore diameter (nm) | BET Surface area (M2 g-1) |
7 | Tergitol | 1.0 | 4.3 | 2.0 | 655 |
15-S-15 | |||||
8 | Tergitol | 5.0 | 3.6 | 2.0 | 465 |
15-S-15 | |||||
9 | Tergitol | 10.0 | 3.9 | 2.0 | 515 |
15-S-15 | |||||
10 | Tergitol | 15.0 | 4.0 | 2.2 | 890 |
15-S-15 | |||||
11 | Tergitol | 25.0 | 5.5 | 2.5 | 700 |
15-S-15 |
*The Material designation is MSU-2. | |||||
Example | Template formula | Amount of Template used.(g) | d100 (nm) | HK pore diameter (nm) | BET Surface area (m2g-1) |
12 | C8Ph(EO)8 | 2.3 | 6.1 | 2.0 | 780 |
13 | C8Ph(EO)10 | 2.7 | 6.2 | 3.5 | 715 |
*The Material designation is MSU-3. | |||||
Example | Template formula b | Amount of template used. (g) | d100 (nm) | HK pore diameter (nm) | BET Surface area (m2g-1) |
14 | (PEO)13- | 5.0 | 7.5 | 8.5 | 1090 |
(PPO)30- | |||||
(PEO)13 | |||||
15 | (PEO)13- | 10.0 | 7.1 | 6.7 | 1150 |
(PPO)30- | |||||
(PEO)13 | |||||
16 | (PEO)13- | 15.0 | 6.1 | 5.8 | 1190 |
(PPO)30- | |||||
(PEO)13 |
Material designation | Example | Template formula | % Metal | d100 (nm) | HK (nm) | BET Surface area (m2g -1 |
Zr-MSU-1 | 18 | C11-15(EO)12 | 5 | 4.9 | 3.0 | 950 |
Ti-MSU-1 | 19 | C11-15(EO)12 | 5 | 4.9 | 2.8 | 940 |
Material designation | Ex. | Template formula | Amount of template used.(g) | d100 (nm) | HK pore diameter (nm) | BET Surface area (m2g-1) |
MSU-3 | 20 | (PEO)13- | 8.6 | 6.3 | 4.2 | 420 |
Alumina | (PPO)30- | |||||
(PEO)13 | ||||||
MSU-1 | 21 | C11-15(EO)9 | 15 | 8.0 | 5.8 | 488 |
Alumina | ||||||
22 | C11-15(EO)12 | 14 | n.o. | 6.8 | 425 | |
23 | C11-15(EO)20 | 14 | n.o. | 7.2 | 530 | |
MSU-4 | 24 | C18Ph(EO)18 | 14 | n.o. | 8.0 | 420 |
Alumina | ||||||
N.O. = Not observed in range 1-20° 2 theta. |
Claims (51)
- A synthetic, semi-crystalline inorganic metal oxide composition having at least one resolved x-ray reflection corresponding to a lattice spacing of 3 to 10 nm, a framework wall thickness of at least about 2 nm, framework confined pores between about 2 and 10 nm, an elementary particle size greater than 500 nm, and a specific surface area of 300 to 1200 square meters per gram.
- A synthetic, semi-crystalline inorganic metal oxide composition having at least one resolved x-ray reflection corresponding to a lattice spacing of 3 to 10 nm, a framework wall thickness of at least about 2 nm, framework confined pores between about 2 and 10 nm, an elementary particle size greater than 500 nm, and a specific surface area of 300 to 1200 square meters per gram prepared by reacting a mixture of a non-ionic poly(alkylene oxide) derived surfactant as a template (N°) and a neutral inorganic metal oxide precursor (I°), followed by hydrolysis and crosslinking of the inorganic oxide precursor to provide the composition.
- The composition of Claim 2 wherein the template is removed from the composition.
- The composition of Claim 2 wherein the surfactant has a terminal hydroxyl group.
- The composition of Claim 2 which has the composition:
nR-EO/AxOy
wherein R-EO is selected from the group consisting of nonionic alkyl polyethylene oxide, alkyl and aryl polyethylene oxide, and polyethylene oxide-polypropylene oxide-polyethylene oxide block co-polymer molecules; A is a metal atom; 0 is oxygen and x and y are the molar stoichiometries of A, and O such that in the composition when calcined, n is about 0, x is about 1, y is about 2. - The composition of Claim 2 which has the desired composition:
nR-EO/AvBwSixDyOz
wherein R-EO is selected from the group consisting of nonionic alkyl polyethylene oxide, alkyl and aryl polyethylene oxide and polyethylene oxide-polypropylene oxide-polyethylene oxide block co-polymer molecules; A is at least one optional trivalent element selected from the group consisting of Al, Ga and Fe; B is at least one optional tetravalent metallic element selected from the group consisting of Ge, Ti, V, Sb and Zr; Si is silicon; D is optional and is a pentavalent or hexavalent element selected from the group consisting of V, W and Mo; O is oxygen and v, w, x, y and z are the molar stoichiometries of A, B, Si, D and O respectively, wherein in the composition when calcined, n is about 0, 0 ≤ v ≤ 2, 0 ≤ w ≤ 1, 0 ≤ x ≤ 1, 0 ≤ y ≤ 2 and 2 ≤ z ≤ 6. - The composition of Claim 2 having X-ray diffraction patterns with at least one reflection corresponding to a lattice of between about 3 to 10 nm.
- The composition of any one of Claims 1 or 2 which after calcination, has an N2, O2 or Ar adsorption-desorption isotherm with a step at P/Po between 0.2 and 0.6 and at least one hysteresis loop.
- The composition of Claim 8 wherein a ratio of textural to framework-confined mesoporosity as determined by the N2, O2 or Ar adsorption isotherm, is about zero.
- The composition of Claim 9 wherein the composition has a specific surface area between 500 and 1200 m2 per gram.
- The composition of Claim 2 wherein a molar ratio of nonionic surfactant to inorganic oxide precursor in the reaction mixture is between 0.05 and 0.2.
- The composition of Claim 1 having an X-ray diffraction pattern selected from the group consisting of Figures 3 and 5.
- The composition of Claim 1 having an N2 adsorption-desorption isotherms and Horvath-Kawazoe pore size distribution selected from the group consisting of Figures 4 and 6.
- The composition of Claim 2 containing the template.
- The composition of Claim 2 in which the template has been removed by calcination.
- The composition of Claim 2 in which the template has been removed through solvent extraction.
- The composition of Claim 1 having an X-ray diffraction pattern as shown in Figure 7.
- The composition of Claim 1 having N2 adsorption-desorption isotherms and Horvath-Kawazoe pore size distribution as shown in Figure 8.
- The composition of Claim 6 containing the template.
- The composition of Claim 6 in which the template has been removed by calcination.
- The composition of Claim 6 in which the template has been removed through solvent extraction.
- The composition of any one of Claims 1 or 2 in which at least one transition metal is dispersed or impregnated in the pores, selected from the group consisting of Ag, Au, Cu, Co, Cr, Ni, Fe, Ir, Mo, Pt, Pd, Sn, Ti, V, W, Zn and Zr.
- The composition of any one of Claims 1 or 2 containing transition metal substituted organic macrocycles in the pores.
- The composition of Claim 2 wherein the surfaces of the composition have been functionalized by an alkyl metal alkoxide precursor represented as M-R(OR) x -1, where M is the metal, x represents available bonding sites on M and where R is alkyl and OR is alkoxide.
- The composition of any one of Claims 2 or 6 wherein the surfaces of the composition upon removal of the template have been functionalized by substitution of the metal alkoxide precursor by a metal carboxylate precursor.
- The composition of any one of Claims 1 or 2 wherein the compositions have surfaces which have been functionalized by reaction of the composition upon removal of the template and calcination with reagents selected from the group consisting of chlorides, fluorides, sylisation and alkylation reagents.
- The composition of Claim 2 wherein the template (N°) is selected from the group consisting of primary, secondary and tertiary fatty alcohol poly(ethoxylates).
- The composition of Claim 2 wherein the nonionic template (N°) is an alkyl phenol poly-(ethoxylates).
- The composition of Claim 2 wherein the nonionic template (N°) is a fatty acid ethoxylate.
- The composition of Claim 2 wherein the nonionic template (N°) is a poly(ethylene oxide-propylene oxide) block co-polymer.
- The composition of Claim 2 wherein the template (N°) is selected from the group consisting of primary and secondary fatty amine poly(ethoxylate).
- The composition of Claim 2 wherein the template (N°) is a fatty acid poly(ethylene oxide-propylene oxide) block co-polymer.
- The composition of Claim 2 wherein the template (N°) is selected from the group consisting of fatty acid alkanolamides and ethoxylates.
- The composition of Claim 2 wherein the template (N°) is selected from the group consisting of sorbitan esters and sorbitan ethoxylates.
- The composition of Claim 2 wherein the template (N°) is a polyamine propoxylate ethoxylate.
- A method for the preparation of a synthetic semi-crystalline inorganic oxide composition which comprises:(a) providing a mixture of (i) a neutral inorganic oxide precursor (I°) containing at least one element selected from the group consisting of di-, tri-, tetra-, penta- and hexavalent elements and mixture thereof; (ii) a non-ionic poly(alkylene oxide) surfactant (S°) as a template; and (iii) a hydrolyzing agent;(b) mixing the solution to form a gel containing the composition;(c) separating at least some of the hydrolyzing agent and the surfactant from the gel; and(d) optionally calcining the composition.
- The method of Claim 36 wherein the gel is prepared by a random order of addition of the neutral template and neutral inorganic oxide precursor.
- A method for the preparation of a synthetic, semi-crystalline inorganic oxide composition which comprises:(a) preparing a solution of a neutral inorganic oxide precursor (I°), containing at least one element selected from the group consisting of di-, tri-, tetra-, penta- and hexavalent elements and mixtures thereof with stirring and optionally aging the inorganic oxide precursor (I°) solution;(b) preparing a homogeneous solution of a nonionic poly(alkylene oxide) surfactant (S°) as a template in a hydrolyzing agent, and optionally in a co-solvent, by stirring it at a temperature between about minus 20° and plus 100°C;(c) mixing of the solutions of steps (a) and (b) at a temperature between about minus 20° and plus 100°C to form a gel which is aged for at least about 30 minutes to form the composition;(d) separating at least some of the hydrolyzing agent and surfactant from the composition; and(e) optionally calcining the composition.
- The method of Claim 38 wherein the neutral precursor is selected from the group consisting of a metal alkoxide, an inorganic complex, a colloidal inorganic oxide solution, an inorganic oxide sol and mixtures thereof.
- The method of Claim 38 wherein said inorganic oxide precursor solution is mixed without aging.
- The method of Claim 38 wherein the template is separated from the composition and as an additional step recycled after step (d).
- The method of Claim 41 wherein the template is separated by extraction with a solvent selected from the group consisting of a neutral organic solvent, water and mixtures thereof.
- The method of Claim 38 wherein in step (a) the solution is a gel with the stirring at a temperature of at least minus 20°C for at least 5 minutes.
- The method of Claim 38 wherein the composition is calcined at about 300° to 1000°C for at least about 30 minutes.
- A method for the preparation of a crystalline inorganic oxide composition which comprises:(a) preparing a homogeneous solution of nonionic poly(ethylene oxide) surfactant as a template (N°) in a lower alkyl alcohol solvent by mixing at ambient temperature;(b) adding an inorganic metal precursor to the solution of step (a) at ambient temperature under stirring for at least 30 minutes to form a homogeneous solution;(c) slowly adding a solution of a hydrolyzing agent to the homogeneous solution to form a gel as a first precipitate in the aqueous solution;(d) aging of the first precipitate with stirring;(e) redispersion of the first precipitate in a lower alkyl alcohol;(f) aging the redispersion under stirring at ambient temperature for 16 to 48 hours to form a second precipitate;(g) separating the aqueous solution, lower alkanol and at least some of the template from the second precipitate by washing once with ethanol; and(h) drying the second precipitate in air at ambient temperature to form the composition.
- The method of Claim 45 wherein the calcining is by combustion in air.
- A method for the preparation of synthetic, semi-crystalline inorganic silicon dioxide composition which comprises:(a) preparing a homogeneous aqueous solution of a nonionic poly(ethylene oxide) derived surfactant template (N°) with mixing at ambient temperature;(b) adding an inorganic silica precursor to the solution of step (a) at ambient temperature with stirring to form a solid, precipitate;(c) aging of the precipitate with stirring at ambient temperature for between 16 and 48 hours;(d) separating the aqueous solution and template from the precipitate followed by washing once with deionized water;(e) drying the precipitated and separated precipitate in air at ambient temperature;(f) heat treating the air dried precipitate in air at least 373°K for at least 16 hours;(g) optionally removing any remaining template by solvent extraction from the heat treated precipitate; and(h) calcining the precipitate to remove any remaining template to cross-link the framework at between 673°K and 923°K in air for at least 4 hours to form the composition.
- The method of Claim 47 wherein the calcining is by combustion in air.
- The method of Claim 45 wherein optionally heat treating the second precipitate to at least 373°K in air for at least 16 hours.
- The method of Claim 45 wherein after step (h) the template is removed by solvent extraction.
- The method of Claim 45 wherein after step (h) the second precipitate is calcined between about 673°K and 923°K in air for at least 4 hours.
Applications Claiming Priority (3)
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US08/465,770 US5622684A (en) | 1995-06-06 | 1995-06-06 | Porous inorganic oxide materials prepared by non-ionic surfactant templating route |
US465770 | 1995-06-06 | ||
PCT/US1996/007574 WO1996039357A1 (en) | 1995-06-06 | 1996-05-24 | Porous inorganic oxide materials prepared by non-ionic surfactant templating route |
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EP0830314A1 EP0830314A1 (en) | 1998-03-25 |
EP0830314A4 EP0830314A4 (en) | 1998-08-26 |
EP0830314B1 true EP0830314B1 (en) | 2002-12-18 |
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US (2) | US5622684A (en) |
EP (1) | EP0830314B1 (en) |
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- 1996-05-24 WO PCT/US1996/007574 patent/WO1996039357A1/en active IP Right Grant
- 1996-05-24 EP EP96916589A patent/EP0830314B1/en not_active Expired - Lifetime
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WO2006128989A1 (en) * | 2005-06-02 | 2006-12-07 | Institut Francais Du Petrole | Mesostructured material with high aluminum content |
FR2886637A1 (en) * | 2005-06-02 | 2006-12-08 | Inst Francais Du Petrole | MESOSTRUCTURE MATERIAL WITH HIGH ALUMINUM CONTENT |
CN101189186B (en) * | 2005-06-02 | 2011-12-14 | 法国石油公司 | Inorganic material that has metal nanoparticles that are trapped in a mesostructured matrix |
Also Published As
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EP0830314A1 (en) | 1998-03-25 |
EP0830314A4 (en) | 1998-08-26 |
DE69625480T2 (en) | 2003-05-15 |
DE69625480D1 (en) | 2003-01-30 |
WO1996039357A1 (en) | 1996-12-12 |
US5622684A (en) | 1997-04-22 |
US5795559A (en) | 1998-08-18 |
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